527682-82-2

Basic information

• Product Name: 4'-methylphenyl 1-thio-α-L-arabinofuranoside
• Synonyms: 4'-methylphenyl 1-thio-α-L-arabinofuranoside
• CAS NO: 527682-82-2
• Molecular Weight: 256.323
• Mol File: 527682-82-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4'-methylphenyl 1-thio-α-L-arabinofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-methylphenyl 1-thio-α-L-arabinofuranoside(527682-82-2)
• EPA Substance Registry System: 4'-methylphenyl 1-thio-α-L-arabinofuranoside(527682-82-2)

Safety Data

• Hazardous Substances Data: 527682-82-2(Hazardous Substances Data)

Upstream product

• 929006-31-5 benzimidazol-2-yl 1-thio-α-L-arabinofuranoside 
• 106-45-6 para-thiocresol 
• 42793-97-5 2,3,5-tri-O-benzoyl-1-O-methyl-α-L-arabinofuranose 
• 13035-61-5 1,2,3,6-tetra-O-acetyl-5-deoxy-α-L-arabino-hexofuranose 

Downstream Products

• 527682-84-4 p-tolyl 2,3-anhydro-5-O-benzoyl-1-thio-α-L-lyxofuranoside 
• 1253375-92-6 p-tolyl 2,3,5-tribenzyl-1-thio-α-L-arabinofuranoside 
• 1451369-72-4 4-methylphenyl 3,5-O-(tetraisopropyldisiloxane-1,3-diyl)-1-thio-α-L-arabinofuranoside 
• 527682-19-5 methyl 5-O-(2,3-anhydro-β-L-lyxofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside 
• 527682-23-1 methyl 5-O-(2,3-anhydro-β-L-lyxofuranosyl)-2,3-di-O-benzyl-α-L-arabinofuranoside 
• 932719-28-3 p-cresyl 2-O-benzyl-3,5-O-(di-tert-butylsilylene)-1-thio-α-L-arabinofuranoside 

Relevant articles and documents

Analysis of Configuration and Conformation of Furanose Ring in Carbohydrate and Nucleoside by Vibrational Circular Dichroism

A reliable and convenient method for determining the configuration and conformation of the furanose ring in carbohydrates and nucleosides by vibrational circular dichroism (VCD) spectroscopy is described. Diastereomeric pairs of several furanose monosacch

Synthesis of a dimer of β-(1,4)-l-arabinosyl-(2 S,4 R)-4-hydroxyproline inspired by art v 1, the major allergen of mugwort

Nα-tert-Butoxycarbonyl-l-trans-4-hydroxyproline allyl ester (Boc-Hyp-OAll) was glycosylated with 2,3,5-tri-O-benzyl-l-arabinose p-cresylthioglycoside in 60% yield with 4:1 β:α stereoselectivity. Deprotection of N- and C-terminii independently gave a prolyl amine and prolyl carboxylate respectively that were coupled under standard conditions with 1-[bis-(dimethylamino)methylene]-1H-1,2,3-triazolo-[4,5,b]-pyridininium hexafluorophosphate 3-oxide (N-HATU) to give the dimer 1 in 46% yield. These results represent the first steps toward the production of homogeneous oligomers to determine the minimal epitope of the Art v 1 allergen.

2,3-Anhydro sugars in glycoside bond synthesis. Highly stereoselective syntheses of oligosaccharides containing α- and β-arabinofuranosyl linkages

The ever-increasing discovery of biologically important events mediated by carbohydrates has generated great interest in the synthesis of oligosaccharides and the development of new methods for glycosidic bond formation. In this paper, we report that 2,3-